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pro vyhledávání: '"Laura eMelchionda"'
Autor:
Laura eMelchionda, Nadirah S Damseh, Bassam Y Abu Libdeh, Alessia eNasca, Orly eElpeleg, Alice eZanolini, Daniele eGhezzi
Publikováno v:
Frontiers in Genetics, Vol 5 (2014)
Isolated complex III (cIII) deficiency is a rare biochemical finding in mitochondrial disorders, mainly associated with mutations in mitochondrial DNA MTCYB gene, encoding cytochrome b, or in assembly factor genes (BCS1L, TTC19, UQCC2 and LYRM7), whe
Externí odkaz:
https://doaj.org/article/fbefafdb8e38451289aae80a1356032c
